Adhesive Propylene Polymer Composition Suitable for Extrusion Coating of Paper Substrates

ABSTRACT

Two-component adhesion composition suitable for extrusion coating paper substrates which comprises a) from 70 to 98 wt % of high melt strength polypropylene (A) with a branching index g′ of 0.9 or less and b) from 2 to 30 wt % of a component (B) selected from the group of (i) maleic anhydride-modified polypropylene (MAPP) (ii) maleic anhydride-modified polypropylene wax (iii) polypropylene homopolymer with high melt flow rate or (iv) ethylene-vinyl acetate-based hot melt adhesive and its use.

The present invention relates to polypropylene-based adhesivecompositions, which are suitable for extrusion coating especially ofpaper substrates.

In general, extrusion coating of substrates such as paper, paperboard,fabrics and metal foils with a thin layer of plastic is practiced on alarge scale. The polymer is extruded first whereby the flux of moltenpolymeric material passes through a flat die to obtain a film a fewmicrons thick, followed by a coating step, whereby the film is laid on asupport and passes on a cooling cylinder. Upon cooling, the polymeradheres to its support.

Low density polyethylene (LDPE) is mainly used in extrusion coatingbecause of the ease in processing although stiffness, barrier propertiesand temperature resistance of LDPE are often not satisfactory.

Polypropylene, also known as propylene polymer, is a well-knowncommercial polymer, which is used for a variety of products, such aspackaging films and moulded shapes.

Commercial propylene polymers exhibit several desirable properties, suchas good heat tolerance and transparency, which make polypropylenepolymers interesting in many application fields.

However, since many polypropylene materials suffer from low meltstrength and low melt extensibility, they show poor processibility inhigh speed extrusion coating.

Further, the adhesion of polypropylene on substrates like paper is notsatisfactory.

For these reasons only a few polypropylene-based systems are availablein the industry for extrusion coating at present.

Many efforts have been undertaken to improve the processing propertiesof polypropylene polymers. The shortcomings during processing havepartially been overcome by the class of high melt strengthpolypropylene. Such polymers are featured by the introduction ofbranchings in the linear polymer backbone. This can be achieved throughpost-reactor treatment, copolymerization with dienes, and throughpolymerization with specific catalysts at high temperatures.

Although these branched polymer types have improved properties, there isstill the desire to improve their adhesion to substrates such as paper.

To improve the adhesion between the substrate and the plastic layerdifferent methods are commonly known, such as ozone treatment of themolten polymer film, flame treatment and corona treatment of thesubstrate or the use of an adhesive layer.

Various further proposals have been made to increase the adhesion ofpropylene polymer layers to different substrates.

For example, U.S. Pat. No. 4,394,485 discloses four component adhesiveblends comprising modified polyolefin resins with improved adhesion topolar substrates such as metal, glass, paper, etc. The blend consists ofhigh density polyethylene (HDPE), LDPE, a polypropylene homo- orcopolymer and a polyethylene polymer grafted with carboxylic acid oracid derivate and can be used in processes like lamination, coextrusion,powder and/or extrusion coating, blow molding, etc. The presence ofpolyethylene components will necessarily limit the thermal stability ofthese compositions.

According to U.S. Pat. No. 4,394,485 adhesion tests have been done byheat seating of compression molded films into substrates, which is notcomparable to the extrusion coating process due the residence time,temperature and thickness of the coating. Nevertheless, an improvedadhesion to rather unporous substrates like polypropylene (PP) andethylene-vinyl alcohol (EVOH) films, and aluminium foil was observed.

WO 00/69982 describes adhesive propylene polymer compositions suitablefor coating substrates, which show improved adhesion to metals withoutthe need for a primer coating or to polymeric substrates, with a primercoating without the need for post heating.

This blend consists of three components comprising (a) 50 to 80 wt % ofan unmodified propylene polymer, which may be a homo- or a copolymer, aheterophasic propylene polymer or mixtures thereof, (b) 10 to 30 wt % ofa high melt strength propylene polymer and (c) 3 to 30 wt % of amodified propylene polymer grafted with an unsaturated compound having apolar group, wherein the total of (a), (b) and (c) is 100%.

U.S. Pat. No. 4,957,968 describes a three component adhesivethermoplastic elastomer blend, which is adherent to metal, glass, wood,polyolefins and polar polymers with no pretreatment or use of otheradhesives.

The three components are (a) a polyolefin modified by a chemicallyreactive functional group, (b) a polymer prepared from one or more ofthe following: ethylene, propylene, butylene, isobutylene,octene-1,4-methyl-pentene-1, hexene-1 and (c) an olefinic elastomer. Forexample such a blend comprises (a) maleic anhydride modifiedpolypropylene, (b) polypropylene and (c) ethylene propylene dienerubber.

WO 00/31181 describes wettable polypropylene compositions comprising upto 85 wt % of unmodified polypropylene and up to 35 wt % of ahydrophilic, polar compound which includes functional sites selectedfrom the group consisting of carboxyl, hydroxyl, ether or estermoieties. For example maleic anhydride-modified polypropylene (MAPP) canbe used as polar compound. To provide permanent wettablity a mixturefrom unmodified polypropylene with e.g. MAPP is treated with hotpotassium hydroxide. The composition can be used for example to achievea wettable polypropylene extrusion coating on paper or paperboard foruse in packaging applications where stiffness and printability isimportant.

Although much development work has been done in the field of adhesivepropylene polymer compositions, there is a continuous need foralternative or improved adhesive propylene polymer compositions, whichcan be used in extrusion coating for paper substrates and which show animproved adhesion to the substrate compared to known propylene polymermaterials, high melt strength propylene polymers and blends thereof.

OBJECT OF THE INVENTION

An object of the invention is therefore to provide polypropylenecompositions, which are particularly suitable for extrusion coating onpaper substrates, having high melt strength and improved adhesion topaper or paperboard without the need of surface treating methods oradditional adhesion layers.

A further object of the invention is the use of the polypropylenecomposition in extrusion coating processes using paper or paperboard assubstrate.

Another object of the present invention is to provide a substrate orarticle which has at least one layer of highly adherent propylenepolymer composition on at least one surface.

SUMMARY OF THE INVENTION

The present invention relates to polypropylene compositions useable forextrusion coating of paper substrates and showing improved adhesion tothe substrate, yielding extrusion coating products of high quality.

Particularly, the present invention deals with two component adhesioncompositions suitable for extrusion coating paper substrates comprisinga blend of high melt strength polypropylene and one component selectedfrom the group of

-   -   (i) maleic anhydride-modified polypropylene (MAPP)    -   (ii) maleic anhydride-modified polypropylene wax    -   (iii) polypropylene homopolymer with high melt flow rate or    -   (iv) ethylene-vinyl acetate-based hot melt adhesive

DETAILED DESCRIPTION OF THE INVENTION

It has now been discovered that the problems and deficiencies relatingto the compositions and blends according to the state of the artregarding insufficient adhesion to paper or paperboard substrates can beavoided or at least significantly decreased with a composition accordingto the present invention. It has been noted that certain combinations ofhigh melt strength polypropylene with special polypropylenes or anethylene-vinyl acetate-based hot melt adhesive meet the objectives.

The two component adhesion composition suitable for extrusion coatingpaper substrates according to the invention comprises:

-   a) from 70 to 98 wt %, preferably 75 to 95 wt % of high melt    strength polypropylene (A) with a branching index g′ of 0.9 or less    and-   b) from 2 to 30 wt %, preferably 5 to 25 wt % of a component (B)    selected from the group of    -   (i) maleic anhydride-modified polypropylene (MAPP)    -   (ii) maleic anhydride-modified polypropylene wax    -   (iii) polypropylene homopolymer with high melt flow rate or    -   (iv) ethylene-vinyl acetate-based hot melt adhesive

Thus the first mandatory component in the present invention is apolypropylene (A) characterized by a certain degree of branching.Possible polypropylenes (A) are so called Y/H-polypropylenes and are forinstance described in EP 0 787 750, i.e. single branched polypropylenetypes (Y polypropylenes having a backbone with a single long side-chainand an architecture resembles a “Y”) and polypropylene types in whichpolymer chains are coupled with a bridging group (an architectureresembles a “H”), as well as multi-branched polypropylenes, i.e. notonly the polypropylene backbone is furnished with a larger number ofside chains (branched polypropylene) but also some of the side chainsthemselves. Such polypropylenes are characterized by rather high meltstrength.

A parameter of the degree of branching is the branching index g′. Thebranching index g′ correlates with the amount of branches of a polymer.The branching index g′ is defined as g′=[IV]_(br)/[IV]_(lin) in which g′is the branching index, [IV_(br)] is the intrinsic viscosity of thebranched polypropylene and [IV]_(lin) is the intrinsic viscosity of thelinear polypropylene having the same weight average molecular weight(within a range of ±10%) as the branched polypropylene. Thereby, a lowg′-value is an indicator for a high branched polymer. In other words, ifthe g′-value decreases, the branching of the polypropylene increases.Reference is made in this context to B. H. Zimm and W. H. Stockmeyer, J.Chem. Phys. 17, 1301 (1949). This document is herewith included byreference.

The intrinsic viscosity needed for determining the branching index g′ ismeasured according to DIN ISO 1628/1, October 1999 (in Decalin at 135°C.).

Thus it is preferred that the branching index g′ of the polypropylene(A) shall be less than 0.9, more preferably equal or less than 0.8. Inanother preferred embodiment the branching index g′ of the polypropylene(A) shall be preferably less than 0.7.

The polypropylene (A) can be a propylene homopolymer or a propylenecopolymer, wherein the homopolymer is preferred.

Accordingly, the homopolymer as well as the copolymer can be a unimodalor multimodal polymer composition.

In a preferred embodiment the polypropylene is preferably unimodal. Inanother preferred embodiment the polypropylene is preferably multimodal,more preferably bimodal.

“Multimodal” or “multimodal distribution” describes a frequencydistribution that has several relative maxima. In particular, theexpression “modality of a polymer” refers to the form of its molecularweight distribution (MWD) curve, i.e. the appearance of the graph of thepolymer weight fraction as a function of its molecular weight. If thepolymer is produced in the sequential step process, i.e. by utilizingreactors coupled in series, and using different conditions in eachreactor, the different polymer fractions produced in the differentreactors each have their own molecular weight distribution which mayconsiderably differ from one another. The molecular weight distributioncurve of the resulting final polymer can be seen at a super-imposing ofthe molecular weight distribution curves of the polymer fraction whichwill, accordingly, show a more distinct maxima, or at least bedistinctively broadened compared with the curves for individualfractions.

A polymer showing such molecular weight distribution curve is calledbimodal or multimodal, respectively.

The expression homopolymer used in the instant invention relates to apolypropylene that consists substantially, i.e. of at least 97 wt %,preferably of at least 99 wt %, and most preferably of at least 99.8 wt% of propylene units. In a preferred embodiment only propylene units inthe propylene homopolymer are detectable. The comonomer content can bedetermined with FT infrared spectroscopy, as described below in theexamples.

In case the polypropylene according to this invention is a propylenecopolymer, it is preferred that the comonomer is ethylene. However, alsoother comonomers known in the art are suitable. Preferably, the totalamount of comonomer, more preferably ethylene, in the propylenecopolymer is up to 15 wt %, more preferably up to 10 wt %.

It is also possible that the polypropylene is a propylene copolymercomprising a polypropylene matrix and an ethylene-propylene rubber(EPR).

The polypropylene matrix can be a homopolymer or a copolymer, morepreferably multimodal, i.e. bimodal, homopolymer or a multimodal, i.e.bimodal, copolymer. In case the polypropylene matrix is a propylenecopolymer, then it is preferred that the comonomer is ethylene orbutene. However, also other comonomers known in the art are suitable.The preferred amount of comonomer, more preferably ethylene, in thepolypropylene matrix is up to 8.00 mol %. In case the propylenecopolymer matrix has ethylene as the comonomer component, it is inparticular preferred that the amount of ethylene in the matrix is up to8.00 mol %, more preferably less than 6.00 mol %. In case the propylenecopolymer matrix has butene as the comonomer component, it is inparticular preferred that the amount of butene in the matrix is up to6.00 mol %, more preferably less than 4.00 mol %.

Preferably, the ethylene-propylene rubber (EPR) in the total propylenecopolymer is up to 60 wt %. More preferably the amount ofethylene-propylene rubber (EPR) in the total propylene copolymer is inthe range of 15 to 60 wt %, still more preferably in the range of 20 to50 wt %.

In addition, it is preferred that the polypropylene being a copolymercomprising a polypropylene matrix and an ethylene-propylene rubber (EPR)has an ethylene-propylene rubber (EPR) with an ethylene-content of up to65 wt %.

The high degree of branching of the polypropylene (A) contributes alsoto its melt strength. Accordingly it is preferred that the polypropylene(A) is further characterized by a melt strength of at least 10 cN at amaximum speed of at least 200 mm/s, more preferably by a melt strengthof at least 20 cN at a maximum speed of at least 200 mm/s, still morepreferably by a melt strength of at least 25 cN at a maximum speed of atleast 200 mm/s, yet more preferably by a melt strength of at least 25 cNat a maximum speed of at least 250 mm/s. The measuring of the meltstrength has been undertaken by a temperature of 200° C. with anacceleration of the melt strand drawn down of 120 mm/sec². The exactmeasuring method is defined in the example section.

Furthermore, it is preferred that the polypropylene has a melt flow rate(MFR) given in a specific range. The melt flow rate mainly depends onthe average molecular weight. This is due to the fact that longmolecules render the material a lower flow tendency than shortmolecules. An increase in molecular weight means a decrease in theMFR-value. The melt flow rate (MFR) is measured in g/10 min of thepolymer discharged through a defined die under specified temperature andpressure conditions and the measure of viscosity of the polymer which,in turn, for each type of polymer is mainly influenced by its molecularweight but also by its degree of branching. The melt flow rate measuredunder a load of 2.16 kg at 230° C. (ISO 1133) is denoted as MFR₂ (230°C.). Accordingly, it is preferred that in the present invention thepolypropylene (A) has an MFR₂ (230° C.) in a range of 0.01 to 100 g/10min, more preferably of 0.10 to 50 g/10 min, still more preferred of1.00 to 25 g/10 min.

Preferably the cross-linked fraction of the polypropylene (A) does notexceed 1.0 wt.-%, even more preferred does not exceed 0.8 wt.-%, stillmore preferred does not exceed 0.5 wt.-% determined as the relativeamount of polymer insoluble in boiling xylene (xylene hot insolublefraction, XHI).

More preferably, the polypropylene of the instant invention isisotactic. Thus the polypropylene according to this invention shall havea rather high pentade concentration, i.e. higher than 90%, morepreferably higher than 92% and most preferably higher than 93%. Inanother preferred embodiment the pentade concentration is higher than95%. The pentade concentration is an indicator for the narrowness in thestereoregularity distribution of the polypropylene.

The high melt strength polypropylene (A) can be preferably furtherdefined by the way obtained.

Accordingly the polypropylene (A) can be the result of treating anunmodified polypropylene (A′) with thermally decomposing radical-formingagents and/or with ionizing radiation, where both treatments mayoptionally be accompanied or followed by a treatment with bi- ormultifunctionally unsaturated monomers, e.g. butadiene, isoprene,dimethylbutadiene or divinylbenzene. A suitable method to obtain thepolypropylene (A) is for instance disclosed in EP 0 879 830 A1 and EP 0890 612 A2. Both documents are herewith included by reference.

The unmodified polypropylene (A′) has preferably a MFR₂ (230° C.) in arange of 0.05 to 45.00 g/10 min. More preferably the MFR₂ (230° C.) isin a range of 0.05 to 35.00 g/10 min in case the unmodifiedpolypropylene (A′) is a homopolymer. On the other hand the MFR₂ (230°C.) is in a range of 0.05 to 45.00 g/10 min in case the unmodifiedpolypropylene (A′) is a copolymer.

Preferably the unmodified polypropylene (A′) comprises 85.0 to 99.9wt.-% of propylene and 0.1 to 15.0 wt % of one or more α-olefins with 2or 4 to 18 carbon atoms, in particular ethylene.

As stated above the unmodified polypropylene (A′) is preferablymultimodal, more preferably bimodal. Accordingly it is preferred thatthe unmodified polypropylene (A′) has a molecular weight distribution(MWD) of 5 to 60, more preferably in the range of 15 to 35.

Moreover the unmodified polypropylene (A′) has preferably a weightaverage molecular weight (M_(w)) of 500,000 to 1,500,000 g/mol, morepreferably in the range of 600,000 to 1,000,000 g/mole. The numberaverage molecular weight (M_(n)) preferably ranges of 25,000 to 100,000g/mol and more preferably of 30,000 to 100,000 g/mol.

The number average molecular weight (Mn) and the weight averagemolecular weight (Mw) as well as the molecular weight distribution (MWD)are determined in the instant invention by size exclusion chromatography(SEC) using Waters Alliance GPCV 2000 instrument with online viscometer.The oven temperature is 140° C. Trichlorobenzene is used as a solvent(ISO 16014).

The peroxide used for the manufacture of polypropylene (A) is preferablya thermally decomposing free radical-forming agent, more preferablyselected from the group consisting of acyl peroxide, alkyl peroxide,hydroperoxide, perester and peroxycarbonate.

The following listed peroxides are in particular preferred:

-   Acyl peroxides: benzoyl peroxide, 4-chlorobenzoyl peroxide,    3-methoxybenzoyl peroxide and/or methyl benzoyl peroxide.-   Alkyl peroxides: allyl t-butyl peroxide,    2,2-bis(t-butylperoxybutane),    1,1-bis(t-butylperoxy)-3,3,5-trimethylcyclohexane,    n-butyl-4,4-bis(t-butylperoxy) valerate,    diisopropylaminomethyl-t-amyl peroxide, dimethylaminomethyl-t-amyl    peroxide, diethylaminomethyl-t-butyl peroxide,    dimethylaminomethyl-t-butyl peroxide,    1,1-di-(t-amylperoxy)cyclohexane, t-amyl peroxide, t-butylcumyl    peroxide, t-butyl peroxide and/or 1-hydroxybutyl n-butyl peroxide.

Peresters and peroxy carbonates: butyl peracetate, cumyl peracetate,cumyl perpropionate, cyclohexyl peracetate, di-t-butyl peradipate,di-t-butyl perazelate, di-t-butyl perglutarate, di-t-butyl perthalate,di-t-butyl persebacate, 4-nitrocumyl perpropionate, 1-phenylethylperbenzoate, phenylethyl nitro-perbenzoate,t-butylbicyclo-(2,2,1)heptane percarboxylate, t-butyl-4-carbomethoxyperbutyrate, t-butylcyclobutane percarboxylate, t-butylcyclohexylperoxycarboxylate, t-butylcyclopentyl percarboxylate,t-butylcyclopropane percarboxylate, t-butyldimethyl percinnamate,t-butyl-2-(2,2-diphenylvinyl) perbenzoate, t-butyl-4-methoxyperbenzoate, t-butylperbenzoate, t-butylcarboxycyclohexane, t-butylpernaphthoate, t-butyl peroxyisopropylcarbonate, t-butyl pertoluate,t-butyl-1-phenylcyclopropyl percarboxylate,t-butyl-2-propylperpentene-2-oate, t-butyl-1-methylcyclopropylpercarboxylate, t-butyl-4-nitrophenyl peracetate, t-butylnitrophenylperoxycarbamate, t-butyl-N-succiimido percarboxylate, t-butylpercrotonate, t-butyl permaleic acid, t-butyl permethacrylate, t-butylperoctoate, t-butyl peroxyisopropylcarbonate, t-butyl perisobutyrate,t-butyl peracrylate and/or t-butyl perpropionate;

or mixtures of these above listed free radical-forming agents.

If present in the process for the manufacture of the polypropylene (A),the (volatile) bifunctional monomers are preferably ethylenicallyunsaturated, multifunctional monomers, like C4 to C10 dienes and/or C7to C10 divinyl compounds. Especially preferred bifunctional monomers arebutadiene, isoprene, dimethylbutadiene and divinylbenzene.

The polypropylene (A) is preferably obtained by a process as describedin EP 0 879 830 A1 and EP 0 890 612 A2. Both documents are herewithincluded by reference. Accordingly the polypropylene is produced by

-   -   (a) mixing        -   (i) a unmodified propylene homopolymer and/or copolymer (A′)            as defined above, preferably a unmodified propylene            homopolymer with a weight average molecular weight (M_(w))            of 500,000 to 1,500,000 g/mol,        -   (ii) from 0.05 to 3 wt.-% based on the components of (i) and            (ii), of a peroxide selected from the group consisting of            acyl peroxide, alkyl peroxide, hydroperoxide, perester and            peroxycarbonate, and        -   (iii) optionally diluted with inert solvents,    -   (b) heating to 30-100° C., preferably to 60-90° C.,    -   (c) sorption of volatile bifunctional monomers, preferably        ethylenically unsaturated, multifunctional monomers, like C4 to        C10 dienes and/or C7 to C10 divinyl compounds, by the unmodified        propylene homopolymer and/or copolymer (A), preferably        unmodified propylene homopolymer (A), from the gas phase at a        temperature of from 20 to 120° C., preferably of from 60 to 100°        C., where the amount of the absorbed bifunctionally unsaturated        monomers is from 0.01 to 10.00 wt.-%, preferably from 0.05 to        2.00 wt.-%, based on the propylene homopolymer (A′),    -   (d) heating and melting the polypropylene composition in an        atmosphere comprising inert gas and/or the volatile bifunctional        monomers, from sorption temperature to 210° C., whereupon the        free-radical generators are decomposed and then    -   (e) heating the melt up to 280° C. in order to remove unreacted        monomers and decomposition products, and    -   (f) agglomerating the melt.

Usual amounts of auxiliary substances, which may range from 0.01 to 2.5%by weight of stabilizers, 0.01 to 1% by weight of processing aids, 0.1to 1% by weight of antistats, 0.2 to 3% by weight of pigments and up to3% by weight of α-nucleating agents, in each case based on the sum ofthe propylene polymers, may be added before step a) and/or f) of themethod and/or before or during step d) and/or e) of the above describedmethod.

The process for producing the modified propylene polymer preferably is acontinuous method, performed in continuous reactors, mixers, kneadersand extruders. Batchwise production of the modified propylene polymerhowever is feasible as well.

Practical sorption times τ of the volatile bifunctional monomers rangefrom 10 to 1000 s, where sorption times τ of 60 to 600 are preferred.

Polypropylene (A) can also be produced in the presence of a metallocenecatalyst, as, for example, described in EP 1 892 264 using a catalystsystem comprising an asymmetric catalyst, whereby the catalyst systemhas a porosity of less than 1.40 ml/g, more preferably less than 1.30ml/g and most preferably less than 1.00 ml/g. The porosity has beenmeasured according to DIN 66135 (N₂). In another preferred embodimentthe porosity is not detectable when determined with the method appliedaccording to DIN 66135 (N₂).

An asymmetric catalyst is a metallocene compound comprising at least twoorganic ligands which differ in their chemical structure. Morepreferably the asymmetric catalyst is a metallocene compound comprisingat least two organic ligands which differ in their chemical structureand the metallocene compound is free of C₂-symmetry and/or any highersymmetry. Preferably the asymmetric metallocene compound comprises onlytwo different organic ligands, still more preferably comprises only twoorganic ligands which are different and linked via a bridge.

Said asymmetric catalyst is preferably a single site catalyst (SSC).

Furthermore it is preferred, that the catalyst system has a surface areaof less than 25 m²/g, yet more preferred less than 20 m²/g, still morepreferred less than 15 m²/g, yet still less than 10 m²/g and mostpreferred less than 5 m²/g. The surface area according to this inventionis measured according to ISO 9277 (N₂).

It is in particular preferred that the catalytic system comprises anasymmetric catalyst, i.e. a catalyst as defined below, and has porositynot detectable when applying the method according to DIN 66135 (N₂) andhas a surface area measured according to ISO 9277 (N₂) less than 5 m²/g.

Preferably the asymmetric catalyst compound, i.e. the asymmetricmetallocene, has the formula (I):(Cp)₂R_(z)MX₂  (i)whereinz is 0 or 1,M is Zr, Hf or Ti, more preferably Zr, andX is independently a monovalent anionic ligand, such as σ-ligandR is a bridging group linking the two Cp ligandsCp is an organic ligand selected from the group consisting ofunsubstituted cyclopentadienyl, unsubstituted indenyl, unsubstitutedtetrahydroindenyl, unsubstituted fluorenyl, substitutedcyclopentadienyl, substituted indenyl, substituted tetrahydroindenyl,and substituted fluorenyl,with the proviso that both Cp-ligands are selected from the above statedgroup and both Cp-ligands have a different chemical structure.

The term “σ-ligand” is understood in the whole description in a knownmanner, i.e. a group bonded to the metal at one or more places via asigma bond. A preferred monovalent anionic ligand is halogen, inparticular chlorine (Cl).

Preferably, the asymmetric catalyst is of formula (I) indicated above,

wherein

M is Zr and

each X is Cl.

Preferably both identical Cp-ligands are substituted.

Preferably both Cp-ligands have different residues to obtain anasymmetric structure.

Preferably, both Cp-ligands are selected from the group consisting ofsubstituted cyclopentadienyl-ring, substituted indenyl-ring, substitutedtetrahydroindenyl-ring, and substituted fluorenyl-ring wherein theCp-ligands differ in the substituents bonded to the rings.

The optional one or more substituent(s) bonded to cyclopentadienyl,indenyl, tetrahydroindenyl, or fluorenyl may be independently selectedfrom a group including halogen, hydrocarbyl (e.g. C₁-C₂₀-alkyl,C₂-C₂₀-alkenyl, C₂-C₂₀-alkynyl, C₃-C₁₂-cycloalkyl, C₆-C₂₀-aryl orC₇-C₂₀-arylalkyl), C₃-C₁₂-cycloalkyl which contains 1, 2, 3 or 4heteroatom(s) in the ring moiety, C₆-C₂₀-heteroaryl, C₁-C₂₀-haloalkyl,—SiR″₃, —OSiR″₃, —SR″, —PR″₂ and —NR″₂, wherein each R″ is independentlya hydrogen or hydrocarbyl, e.g. C₁-C₂₀-alkyl, C₂-C₂₀-alkenyl,C₂-C₂₀-alkynyl, C₃-C₁₂-cycloalkyl or C₆-C₂₀-aryl.

More preferably both Cp-ligands are indenyl moieties wherein eachindenyl moiety bear one or two substituents as defined above. Morepreferably each Cp-ligand is an indenyl moiety bearing two substituentsas defined above, with the proviso that the substituents are chosen insuch are manner that both Cp-ligands are of different chemicalstructure, i.e. both Cp-ligands differ at least in one substituentbonded to the indenyl moiety, in particular differ in the substituentbonded to the five member ring of the indenyl moiety.

Still more preferably both Cp are indenyl moieties wherein the indenylmoieties comprise at least at the five membered ring of the indenylmoiety, more preferably at 2-position, a substituent selected from thegroup consisting of alkyl, such as C₁-C₆ alkyl, e.g. methyl, ethyl,isopropyl, and trialkyloxysiloxy, wherein each alkyl is independentlyselected from C₁-C₆ alkyl, such as methyl or ethyl, with proviso thatthe indenyl moieties of both Cp must chemically differ from each other,i.e. the indenyl moieties of both Cp comprise different substituents.

Still more preferred both Cp are indenyl moieties wherein the indenylmoieties comprise at least at the six membered ring of the indenylmoiety, more preferably at 4-position, a substituent selected from thegroup consisting of a C₆-C₂₀ aromatic ring moiety, such as phenyl ornaphthyl, preferably phenyl, which is optionally substituted with one ormore substituents, such as C₁-C₆ alkyl, and a heteroaromatic ringmoiety, with proviso that the indenyl moieties of both Cp mustchemically differ from each other, i.e. the indenyl moieties of both Cpcomprise different substituents.

Yet more preferably both Cp are indenyl moieties wherein the indenylmoieties comprise at the five membered ring of the indenyl moiety, morepreferably at 2-position, a substituent and at the six membered ring ofthe indenyl moiety, more preferably at 4-position, a furthersubstituent, wherein the substituent of the five membered ring isselected from the group consisting of alkyl, such as C₁-C₈ alkyl, e.g.methyl, ethyl, isopropyl, and trialkyloxysiloxy, wherein each alkyl isindependently selected from C₁-C₆ alkyl, such as methyl or ethyl, andthe further substituent of the six membered ring is selected from thegroup consisting of a C₆-C₂₀ aromatic ring moiety, such as phenyl ornaphthyl, preferably phenyl, which is optionally substituted with one ormore substituents, such as C₁-C₆ alkyl, and a heteroaromatic ringmoiety, with proviso that the indenyl moieties of both Cp mustchemically differ from each other, i.e. the indenyl moieties of both Cpcomprise different substituents. It is in particular preferred that bothCp are idenyl rings comprising two substituents each and differ in thesubstituents bonded to the five membered ring of the idenyl rings.

Concerning the moiety “R” it is preferred that “R” has the formula (II)—Y(R′)₂—  (II)whereinY is C, Si or Ge, andR′ is C₁ to C₂₀ alkyl, C₆-C₁₂ aryl, or C₇-C₁₂ arylalkyl ortrimethylsilyl.

In case both Cp-ligands of the asymmetric catalyst as defined above, inparticular case of two indenyl moieties, are linked with a bridge memberR, the bridge member R is typically placed at 1-position. The bridgemember R may contain one or more bridge atoms selected from e.g. C, Siand/or Ge, preferably from C and/or Si. One preferable bridge R is—Si(R′)₂—, wherein R′ is selected independently from one or more of e.g.trimethylsilyl, C₁-C₁₀ alkyl, C₁-C₂₀ alkyl, such as C₆-C₁₂ aryl, orC₇-C₄₀, such as C₇-C₁₂ arylalkyl, wherein alkyl as such or as part ofarylalkyl is preferably C₁-C₆ alkyl, such as ethyl or methyl, preferablymethyl, and aryl is preferably phenyl. The bridge —Si(R′)₂— ispreferably e.g. —Si(C₁-C₆ alkyl)₂-, —Si(phenyl)₂ or —Si(C₁-C₆alkyl)(phenyl)-, such as —Si(Me)₂-.

In a preferred embodiment the asymmetric catalyst, i.e. the asymmetricmetallocene, is defined by the formula (III)(Cp)₂R₁ZrCl₂  (III)whereinboth Cp coordinate to M and are selected from the group consisting ofunsubstituted cyclopentadienyl, unsubstituted indenyl, unsubstitutedtetrahydroindenyl, unsubstituted fluorenyl, substitutedcyclopentadienyl, substituted indenyl, substituted tetrahydroindenyl,and substituted fluorenyl,with the proviso that both Cp-ligands are of different chemicalstructure, and R is a bridging group linking two ligands L,wherein R is defined by the formula (II)—Y(R′)₂—  (II)whereinY is C, Si or Ge, andR′ is C₁ to C₂₀ alkyl, C₆-C₁₂ aryl, or C₇-C₁₂ arylalkyl.

More preferably the asymmetric catalyst is defined by the formula (III),wherein both Cp are selected from the group consisting of substitutedcyclopentadienyl, substituted indenyl, substituted tetrahydroindenyl,and substituted fluorenyl.

Yet more preferably the asymmetric catalyst is defined by the formula(III), wherein both Cp are selected from the group consisting ofsubstituted cyclopentadienyl, substituted indenyl, substitutedtetrahydroindenyl, and substituted fluorenyl

with the proviso that both Cp-ligands differ in the substituents, i.e.the substituents as defined above, bonded to cyclopentadienyl, indenyl,tetrahydroindenyl, or fluorenyl.

Still more preferably the asymmetric catalyst is defined by the formula(III), wherein both Cp are indenyl and both indenyl differ in onesubstituent, i.e. in a substituent as defined above bonded to the fivemember ring of indenyl.

It is in particular preferred that the asymmetric catalyst is anon-silica supported catalyst as defined above, in particular ametallocene catalyst as defined above.

In a preferred embodiment the asymmetric catalyst is dimethylsilyl[(2-methyl-(4′-tert.butyl)-4-phenyl-indenyl)(2-isopropyl-(4′-tert.butyl)-4-phenyl-indenyl)]zirkoniumdichloride (IUPAC: dimethylsilandiyl[(2-methyl-(4′-tert.butyl)-4-phenyl-indenyl)(2-isopropyl-(4′-tert.butyl)-4-phenyl-indenyl)]zirkoniumdichloride). More preferred said asymmetric catalyst is not silicasupported.

The above described asymmetric catalyst components are preparedaccording to the methods described in WO 01/48034.

It is in particular preferred that the asymmetric catalyst system isobtained by the emulsion solidification technology as described in WO03/051934. This document is herewith included in its entirety byreference. Hence the asymmetric catalyst is preferably in the form ofsolid catalyst particles, obtainable by a process comprising the stepsof

-   -   a) preparing a solution of one or more asymmetric catalyst        components;    -   b) dispersing said solution in a solvent immiscible therewith to        form an emulsion in which said one or more catalyst components        are present in the droplets of the dispersed phase,    -   c) solidifying said dispersed phase to convert said droplets to        solid particles and optionally recovering said particles to        obtain said catalyst.

Preferably a solvent, more preferably an organic solvent, is used toform said solution. Still more preferably the organic solvent isselected from the group consisting of a linear alkane, cyclic alkane,linear alkene, cyclic alkene, aromatic hydrocarbon andhalogen-containing hydrocarbon.

Moreover the immiscible solvent forming the continuous phase is an inertsolvent, more preferably the immiscible solvent comprises a fluorinatedorganic solvent and/or a functionalized derivative thereof, still morepreferably the immiscible solvent comprises a semi-, highly- orperfluorinated hydrocarbon and/or a functionalized derivative thereof.It is in particular preferred, that said immiscible solvent comprises aperfluorohydrocarbon or a functionalized derivative thereof, preferablyC₃-C₃₀ pertluoroalkanes, -alkenes or -cycloalkanes, more preferredC₄-C₁₀ perfluoro-alkanes, -alkenes or -cycloalkanes, particularlypreferred perfluorohexane, perfluoroheptane, perfluorooctane orperfluoro (methylcyclohexane) or a mixture thereof.

Furthermore it is preferred that the emulsion comprising said continuousphase and said dispersed phase is a bi- or multiphasic system as knownin the art. An emulsifier may be used for forming the emulsion. Afterthe formation of the emulsion system, said catalyst is formed in situfrom catalyst components in said solution.

In principle, the emulsifying agent may be any suitable agent whichcontributes to the formation and/or stabilization of the emulsion andwhich does not have any adverse effect on the catalytic activity of thecatalyst. The emulsifying agent may e.g. be a surfactant based onhydrocarbons optionally interrupted with (a) heteroatom(s), preferablyhalogenated hydrocarbons optionally having a functional group,preferably semi-, highly- or perfluorinated hydrocarbons as known in theart. Alternatively, the emulsifying agent may be prepared during theemulsion preparation, e.g. by reacting a surfactant precursor with acompound of the catalyst solution. Said surfactant precursor may be ahalogenated hydrocarbon with at least one functional group, e.g. ahighly fluorinated C₁ to C₃₀ alcohol, which reacts e.g. with acocatalyst component, such as aluminoxane.

In principle any solidification method can be used for forming the solidparticles from the dispersed droplets. According to one preferableembodiment the solidification is effected by a temperature changetreatment. Hence the emulsion subjected to gradual temperature change ofup to 10° C./min, preferably 0.5 to 6° C./min and more preferably 1 to5° C./min. Even more preferred the emulsion is subjected to atemperature change of more than 40° C., preferably more than 50° C.within less than 10 seconds, preferably less than 6 seconds.

The recovered particles have preferably an average size range of 5 to200 μm, more preferably 10 to 100 μm.

Moreover, the form of solidified particles have preferably a sphericalshape, a predetermined particles size distribution and a surface area asmentioned above of preferably less than 25 m²/g, still more preferablyless than 20 m²/g, yet more preferably less than 15 m²/g, yet still morepreferably less than 10 m²/g and most preferably less than 5 m²/g,wherein said particles are obtained by the process as described above.

For further details, embodiments and examples of the continuous anddispersed phase system, emulsion formation method, emulsifying agent andsolidification methods reference is made e.g. to the above citedinternational patent application WO 03/051934.

As mentioned above the catalyst system may further comprise an activatoras a cocatalyst, as described in WO 03/051934, which is enclosed hereinwith reference.

Preferred as cocatalysts for metallocenes and non-metallocenes, ifdesired, are the aluminoxanes, in particular theC₁-C₁₀-alkylaluminoxanes, most particularly methylaluminoxane (MAO).Such aluminoxanes can be used as the sole cocatalyst or together withother cocatalyst(s). Thus besides or in addition to aluminoxanes, othercation complex forming catalysts activators can be used. Said activatorsare commercially available or can be prepared according to the prior artliterature.

Further aluminoxane cocatalysts are described i.a. in WO 94/28034 whichis incorporated herein by reference. These are linear or cyclicoligomers of having up to 40, preferably 3 to 20, —(Al(R′″)O)— repeatunits (wherein R′″ is hydrogen, C₁-C₁₀-alkyl (preferably methyl) orC₆-C₁₈-aryl or mixtures thereof).

The use and amounts of such activators are within the skills of anexpert in the field. As an example, with the boron activators, 5:1 to1:5, preferably 2:1 to 1:2, such as 1:1, ratio of the transition metalto boron activator may be used. In case of preferred aluminoxanes, suchas methylaluminumoxane (MAO), the amount of Al, provided by aluminoxane,can be chosen to provide a molar ratio of Al:transition metal e.g. inthe range of 1 to 10 000, suitably 5 to 8000, preferably 10 to 7000,e.g. 100 to 4000, such as 1000 to 3000. Typically in case of solid(heterogeneous) catalyst the ratio is preferably below 500.

The quantity of cocatalyst to be employed in the catalyst of theinvention is thus variable, and depends on the conditions and theparticular transition metal compound chosen in a manner well known to aperson skilled in the art.

Any additional components to be contained in the solution comprising theorganotransition compound may be added to said solution before or,alternatively, after the dispersing step.

The process for producing polypropylene (A) using the above definedmetallocene catalyst is a multi-stage process.

Multistage processes include also bulk/gas phase reactors known asmultizone gas phase reactors for producing multimodal propylene polymer.

A preferred multistage process is a “loop-gas phase”-process, such asdeveloped by Borealis A/S, Denmark (known as BORSTAR® technology)described e.g. in patent literature, such as in EP 0 887 379 or in WO92/12182.

Multimodal polymers can be produced according to several processes whichare described, e.g. in WO 92/12182, EP 0 887 379 and WO 97/22633.

A multimodal polypropylene (A) is produced preferably in a multi-stageprocess in a multi-stage reaction sequence as described in WO 92/12182.The contents of this document are included herein by reference.

The second component of the composition can be selected from the groupof

-   -   (i) maleic anhydride-modified polypropylene (MAPP)    -   (ii) maleic anhydride-modified polypropylene wax    -   (iii) polypropylene homopolymer with high melt flow rate or    -   (iv) ethylene-vinyl acetate-based hot melt adhesive        ad (i) maleic anhydride-modified polypropylene (MAPP):

The graft modification of polymers with various olefinically unsaturatedmonomers is well known in the art and numerous commercially availablegraft modified maleic anhydride polymers are available.

The graft-modified polypropylene (i) used in the present invention is apolypropylene modified by partially or wholly grafting with maleicanhydride.

The propylene used for graft modification is a homopolymer of propyleneand/or a random copolymer of propylene and an alpha-olefin containingconstituent units derived from the alpha-olefin other than propylene inamounts of not more than 10% by mole based on 100% by mol of the totalof constituent units derived from propylene and constituent unitsderived from an alpha-olefin other than propylene. Ethylene and/or analpha-olefin having 4 to 20 carbon atoms, including 1-butene, 1-pentene,1-hexene, 1-heptene, 1-octene, 1-nonene, 1-decene and4-methyl-1-pentene, are used as the alpha-olefin in the propylene,either singly or in combination of two or more kinds.

In the propylene/alpha-olefin random copolymer, constituent unitsderived from propylene are contained in amounts of not less than 90% bymol, usually 90 to 99% by mol, preferably not less than 96% by mol, andconstituent units derived from ethylene or an alpha-olefin of 4 to 20carbon atoms are contained in amounts of not more than 10% by mol,usually 1 to 10% by mol, preferably not more than 6% by mol.

Examples of propylene/alpha-olefin random copolymers include apropylene/ethylene copolymer, a propylene/1-butene copolymer, apropylene/ethylene/1-butene copolymer and a propylene/ethylene/1-octenecopolymer.

Preferably a random copolymer of propylene with ethylene is used.

The production method of the polypropylene used for graft modificationin the present invention is not particularly limited. The polypropylenemay be produced by using well-known catalysts such as Ziegler-Nattacatalysts or a metallocene catalyst with well-known processes.

In the modified polypropylene, a part or the whole of propylene (apropylene homopolymer or a propylenelalpha-olefin random copolymer) isgraft modified with maleic anhydride in an amount of preferably 10⁻⁸ to10⁻² g equivalent, more preferably 10⁻⁷ to 10⁻³ g equivalent, based on 1g of the polypropylene before the graft modification. That is, themodified polypropylene may partly include unmodified polypropylene. Whenthe modified polypropylene for use in the invention contains unmodifiedpolypropylene, the content of the unmodified polypropylene is desired tobe not more than 95 parts per weight, usually 85 to 40 parts by weight,based on 100 parts by weight of the total of the graft modifiedpolypropylene and the unmodified polypropylene.

The method of graft modification of the propylene with maleic anhydrideis not particularly limited and can be carried out by well-known graftpolymerization methods such as a solvent method or a melt kneadingmethod. For example, a method of performing graft reaction by adding thegraft monomer maleic anhydride to a molten polymer or a method ofperforming graft reaction by dissolving a polymer in a solvent to make asolution to which the graft monomer is added may be employed.

When the graft polymerization is carried out in the presence of aradical initiator in the above processes, the graft monomer maleicanhydride can be efficiently graft polymerized. In this case, theradical initiator is used in an amount of usually 0.001 to 1 part perweight based on 100 parts per weight of the polypropylene. The radicalinitiators used herein are, for example, an organic peroxide or an azocompound.

Specific examples of the radical initiators include benzoyl peroxide,lauroyl peroxide, dichlorobenzoy peroxide, dicumyl peroxide, di-t-butylperoxide,2,5-dimethyl-2,5-di(t-butylperoxide)hexyne-3,2,5-dimethyl-2,5-di-(t-butylperoxide)-hexane,1,4-bis(t-butylperoxyisopropyle)benzene, azobisisobutyronitrile, etc.

The reaction temperature of the graft polymerization reaction using aradical initiator or the graft polymerization using no radical initiatoris set in the range of usually 60 to 350° C., preferably 150° C. to 300°C.

The content of the maleic anhydride can be easily controlled, forexample, by suitable selection of the grafting conditions.

The content of maleic anhydride in the graft-modified polypropylene usedin the present invention is in the range of 0.001 to 10 wt %, preferably0.01 to 5 wt %, more preferably 0.02 to 4 wt %.

The graft modified polypropylene has normally a melt flow rate (MFR)measured according to ISO 1133 at 230° C. under a load of 2.16 kg of0.01 to 1000 g/10 min, preferably 0.1 to 500 g/10 min, more preferably1.0 to 50 g/10 min.

The anhydride modified polypropylene used in the present invention ispreferably a modification product obtained by grafting maleic anhydrideon a homopolymer of propylene or a propylene/ethylene random copolymer.More preferably the MAPP used according to the invention is a maleicanhydride modified propylene/ethylene random copolymer.

Examples of commercially available modified polypropylene products thatcan suitably be employed in the present invention are Priex® 25097 bySolvay, Hercoprime™ G-211 by Himont Inc., Admer® AT2059E by MitsuiChemicals, Bynel® 50E803 by DuPont, Exxelor PO 1020 by ExxonMobil,Polybond® 3200 by Crompton, Scona® TPPP 2112 F by Kometra, and the like.

Ad (ii) maleic anhydride-modified polypropylene wax

Suitable maleic anhydride-modified propylene waxes include homopolymersof propylene or copolymers of propylene with ethylene or one or more1-olefins produced in the presence of a Ziegler-Natta or metallocenecatalyst and subsequently grafted with maleic anhydride.

1-olefins used include linear or branched olefins having 4 to 18 carbonatoms, preferably 4 to 10 carbon atoms. These olefins may have anaromatic substitution which is in conjugation with the olefinic doublebond. Examples of such compounds are 1-butene, 1-hexene, 1 octene or1-octadecen and also styrene. Preference is given to propylenehomopolymers or propylene copolymers with ethylene.

Especially suitable modified polypropylene waxes are those having asoftening point Ts (ring/ball) from 85 to 165° C., a melt viscosity,measured at a temperature 10° C. above Ts, of between 20 and 40 000mPa·s, preferably between 50 and 10 000 mPa·s and a density at 23° C.between 0.89 and 0.96 g/cm³, preferably between 0.91 and 0.94 g/cm³.

The weight average molecular weight (Mw) of the polypropylene waxes usedfor being grafted is preferably of less than 10.000 g/mol, morepreferably in the range of 500 to 10.000 g/mol, still more preferably inthe range of 1.000 to 9.000 g/mol.

The fraction of the polar graft comonomer (maleic anhydride), based ongrafted polypropylene wax is preferably 0.1 wt % to 20 wt %.

In a preferred embodiment of the present invention the graftedpolypropylene wax has a high degree of grafting, i.e. high content ofmaleic anhydride in the graft-modified polypropylene wax used in thepresent invention.

The acid number of the modified propylene wax is from 0.5 to 120 mgKOH/g, preferably from 1 to 60 mg KOH/g, more preferably from 2 to 40 mgKOH/g.

The acid number is defined as the number of milligrams of KOH which arerequired to neutralize one gram of sample. Acid numbers were obtained bytitrating weighed samples dissolved in refluxing-xylene with methanolicpotassium hydroxide using phenolphthalein as an indicator. End pointswere taken when the pink color of the indicator remained 10 seconds.

The synthesis of the unmodified, i.e. nonpolar, starting waxes by meansof catalysts of the Ziegler or metallocene type is known from numerousdocuments. Thus, for example, DE-A-2329641 discloses a process by meansof which α-olefins can be polymerized in a direct polymerizationreaction using Ziegler catalysts to give homopolymer or copolymer waxes.DE-A-3148229 describes the preparation of highly crystallinepolypropylene waxes by polymerization likewise using titanium-containingcatalysts; the same in EP-A480190. In addition, propylene homopolymerand copolymer waxes are also obtainable using metallocene catalysts(e.g. U.S. Pat. No. 6,331,590, EP-A-321 852, EP-A-384 264, EP-A416 566or EP 571 882).

Suitable starting materials are low molecular weight propylenehomopolymers prepared using Ziegler or metallocene catalysts and havingmelt viscosities, measured at a temperature 10° C. above Ts, of from 20to 50 000 mPa·s. The softening points (ring/ball) of such waxes aregenerally from 90 to 165° C. Suitable waxes are both highly crystallineproducts having a high proportion of isotactic or syndiotacticstructures and those having a low crystallinity and a predominantlyatactic structure. The degree of crystallinity of propylene homopolymerscan be varied within wide limits in a known manner by appropriateselection of the catalyst used for the polymerization and by means ofthe polymerization conditions. This applies particularly when usingmetallocene catalyst systems.

Further suitable starting materials are propylene copolymer waxes whichare prepared using Ziegler or metallocene catalysts and comprise notonly propylene but also varying amounts of other olefins, for exampleethylene or higher α-olefins having a chain length range of C₄-C₃₀,where the comonomer units can be distributed either predominantlyrandomly or predominantly in blocks between isotactic, syndiotactic orpartially atactic polypropylene sequences. Such waxes have softeningpoints (ring/ball) of generally from about 90 to 165° C.

Preferably unmodified polypropylene waxes prepared in the presence of ametallocene catalyst are used for being grafted with maleic acid.

The grafting process can be performed as described for component (i),according to well-known processes. For example, grafting with maleicanhydride may be performed for example according to U.S. Pat. No.5,998,547, U.S. Pat. No. 6,569,950 or EP 0 941 257.

The reaction of the polypropylene wax with maleic anhydride can becarried out either continuously or batchwise. In the batchwiseprocedure, the wax is heated to a temperature above its softening pointand maleic anhydride and a peroxide, as described above, are introducedinto the melt while stirring, either continuously over an appropriateperiod of time or in one or more portions, if desired under a blanket ofinert gas. The reaction temperature is above the softening point of thewax, preferably from 100 to 200° C., particularly preferably from 130 to180° C. After metering-in is complete, the mixture can be left to reactfurther at the same temperature or a different temperature, if desiredafter addition of a further amount of peroxide. Volatile componentsformed during the reaction or excess volatile starting components can,for example, be distilled off under reduced pressure or be removed bystripping with inert gas.

Examples of commercially available modified polypropylene products thatcan suitably be employed in the present invention are Licocene® PP MA7452, Licocene® PP MA 6252 TP, Licocene® PP MA 6452, Licocene® PP MA1332 TP, Licocene® PP MA 1452 all by Clariant, Epolene E-43 by Eastman,and the like.

(iii) polypropylene homopolymer with high melt flow rate

According to the present invention polypropylene homopolymers with highmelt flow rate can also be used as component B.

The polymers that can be suitably be employed have a melt flow rate(MFR) measured according to ISO 1133 at 230° C. under a load of 2.16 kgof from 50 to 3000 g/10 min, preferably from 100 to 2000 g/10 min, morepreferably from 200 to 1500 g/10 min.

The expression homopolymer used in the instant invention relates to apolypropylene that consists substantially, i.e. of at least 97 wt %,preferably of at least 99 wt %, and most preferably of at least 99.8 wt% of propylene units. In a preferred embodiment only propylene units inthe propylene homopolymer are detectable. The comonomer content can bedetermined with FT infrared spectroscopy, as described below in theexamples.

The high melt flow rate polypropylenes used according to the inventioncan be produced directly in a polymerization reactor by well knownprocesses, described in several patent applications (for example in EP 0320 150, EP 0 480 190, EP 0 622 380, EP 1 303 547, EP 1 538 167, EP 1783 145, WO 2007/140019, etc.).

Alternatively the high melt flow rate polypropylenes used according tothe invention can be obtained by controlled rheology (CR) techniques,including, e.g., visbreaking, which means that a polymer, having lowmelt flow rate, is subjected to a post-reactor treatment, wherein thepolymer molecules are subjected to controlled scission in molten state.The scission may be carried out by mechanical shearing, radiation andoxidation or chemically with peroxy compounds.

Preferably controlled rheology treatments are carried out using organicperoxides.

The process of visbreaking a propylene polymer material is well known tothose skilled in the art and is described in several patent applications(for example in U.S. Pat. No. 3,940,379, U.S. Pat. No. 4,951,589, U.S.Pat. No. 4,282,076, U.S. Pat. No. 5,250,631, EP 0 462 574, WO 02/096986,WO 2004/113438

The polymer used as starting compound for the controlled rheologytreatment may be produced by any polymerisation process known in theart.

The polymerisation process may be a continuous process or a batchprocess utilising known methods and operating in liquid phase,optionally in the presence of an inert diluent, or in gas phase or bymixed liquid-gas techniques. The process is preferably carried out inthe presence of a stereospecific catalyst system.

As catalyst any ordinary stereospecific Ziegler-Natta catalysts or anymetallocene catalyst capable of catalysing the formation of a propylenepolymer can be used.

In addition, examples of commercially available modified polypropyleneproducts that can suitably be employed in the present invention areBorflow™ HL504FB, HL508FB or HL512FB all by Borealis, Metocene MF650 byBasell Polyolefins, Marlex® HGZ-1200 by Phillips Sumika PolypropyleneCompany, Escorene™ PP3505 and PP3746 all by ExxonMobile, EOD 96-36 and3960X by Fina, Valtec grades like HH442H, HH441, PF008, PF017, etc. byLyondellBasell etc.

(iv) ethylene-vinyl acetate-based hot melt adhesive

A hot melt adhesive is generally manufactured from a mixture of threecomponents: a thermoplastic resin, a tackifying agent, and paraffin or amicrocrystalline polymeric wax. The thermoplastic resins commonly usedin compositions for the manufacture of hot melt adhesives have includedcopolymers of ethylene and vinyl esters, particularly vinyl acetate, orcopolymers of ethylene and alkyl acrylates, particularly ethyl acrylateand butyl acrylate.

According to the present invention hot melt adhesives based onethylene-vinyl acetate copolymers can be used as component B

Various formulations including ethylene-vinyl acetate (EVA) copolymersare known in the art.

Ethylene-vinyl acetate (EVA) copolymers are conventionally regarded asthose copolymers of ethylene and vinyl acetate where the weightpercentage of ethylene in the polymer molecule exceeds that of the vinylacetate.

The ethylene-vinyl acetate copolymers (EVA) useful herein are thosecontaining at least about 15 to 45 wt % vinyl acetate and having a meltindex (ISO 1133, 190° C., 2.16 kg) in the range of 2 to 2500 g/10 min.The EVA copolymers will preferably comprise less than 40 weight percentvinyl acetate (VA), although EVA copolymers are nowadays available witha vinyl acetate content of above 50 wt %

Useful commercially available ethylene-vinyl acetate copolymers are forexample ATEVA® grades from AT Plastics Inc., Brampton, Ontario,Escruene® grades from ExxonMobile, Elvax® grades from Dupont, Evatane®grades, for example supplied by Atofina, and the like.

Useful commercially available hot melt adhesives based on ethylene-vinylacetate copolymers that can suitably be employed in the presentinvention are for example Sitomelt® grades like K 608/1 from Kiilto OY,Quicklock Hotmelt CH 155 supplied by Chemline India Ltd., 3M™ Jet-melt™hot melt adhesive grades, etc.

The two component adhesion compositions according to the presentinvention comprise a) 70 to 98 wt % of component (A), described indetail above and b) 2 to 30 wt % of component (B), described in detailabove.

Preferably the two component adhesion compositions according to thepresent invention comprise a) 75 to 95 wt % of component (A) and b) 5 to25 wt % of component (B).

As component (B) preferably one compound selected from the group of

-   -   (i) maleic anhydride-modified polypropylene (MAPP)    -   (ii) maleic anhydride-modified polypropylene wax or    -   (iv) ethylene-vinylacetat based hot melt adhesive        all described in detail above, is used.

More preferably component (B) is (i) a maleic anhydride-modifiedpolypropylene (MAPP) or (ii) a maleic anhydride-modified polypropylenewax and still more preferably component (B) is a maleicanhydride-modified polypropylene wax.

The adhesive composition in accordance with the present invention mayfurthermore comprise small amounts of additional, conventionalcomponents (additives), commonly used and well known in the adhesiveart. The type and amount of such additives can be selected by theskilled person on the basis of the general knowledge in the art.Typically these additive do not amount to more than 5 wt.-% (in total),based on the adhesive composition.

The adhesive composition may be prepared in a usual manner, includingblending the individual components using appropriate devices, such askneaders and extruders. Thus the highly adhesive composition of thepresent invention may be prepared by mixing the two components andoptionally one or more additives, as described above, to form a blendand then melt kneading the resulting mixture.

The melt-kneading may be carried out using a kneading machine, such as amixing roll, a Branbury mixer, a kneader, or a single-screw ortwin-screw extruder.

The adhesive composition according to the present invention hasparticular utility as a coating for paper substrates.

Any types of papers conventionally known in the art for preparing coatedpapers can be used, such as but not limited to kraft paper, natural orsynthetic pulp paper, paper board, liner board and the like. The papermay further be bleached and/or coated.

The adhesive composition in accordance with the present invention is inparticular suitable for coating by extrusion processes.

The extrusion coating process may be carried out using conventionalextrusion coating techniques.

Hence, the adhesive composition according to the present invention isfed, typically in the form of pellets, optionally containing additives,to an extruding device. From the extruder the polymer melt is passedpreferably through a flat die to the substrate to be coated. Due to thedistance between the die lip and the nip, the molten plastic is oxidizedin the air for a short period, usually leading to an improved adhesionbetween the coating and the substrate. The coated substrate is cooled ona chill roll, after which it is passed to edge trimmers and wound up.The width of the line may vary between, for example, 500 to 1500 mm,e.g. 800 to 1100 mm, with a line speed of up to 1000 m/min, for instance300 to 800 m/min. The temperature of the polymer melt is typicallybetween 275 and 330° C. The polypropylene of the invention can beextruded onto the substrate as a monolayer coating or as one layer incoextrusion. In a multilayer extrusion coating, the other layers maycomprise any polymer resin having the desired properties andprocessability.

Therefore, a further object of the invention is the use of thepolypropylene composition in extrusion coating processes using paper, asdefined above, as substrate.

The composition of the present invention is highly adhesive and thusnone of the methods commonly known in the art to improve adhesionbetween the paper substrate and the polypropylene layer produced fromthe composition according to the invention, such as ozone treatment ofthe molten polymer film, corona treatment of the substrate and use of acoextruded adhesion layer need to be applied.

Nevertheless it is possible to perform ozone and/or corona treatment ina know way, if desired or necessary.

The main end-uses for extrusion coated products obtained by using theadhesive composition according to the invention are in packagingapplications, like liquid packaging for milk, juice, wine or otherliquids, flexible packaging for meat, cheese and medical products, rigidpackaging like detergent cartons, cup and plate boards for oven ormicrowave use or sterilizable food packaging, but also for photographicpaper or industrial applications like paper reel and ream wraps.

The present invention, as outlined above, therefore also provides asubstrate, respectively article which has at least one layer of highlyadherent propylene polymer composition according to the invention on atleast one surface.

Furthermore the present invention is also directed to the use of theinventive article as packaging material, in particular as a packagingmaterial for food and/or medical products.

In the following, the present invention is described by way of examples.

Definitions/Measuring Methods

The following definitions of terms and determination methods apply forthe above general description of the invention as well as to the belowexamples unless otherwise defined.

Number average molecular weight (M_(n)), weight average molecular weight(M_(w)) and molecular weight distribution (MWD) are determined by sizeexclusion chromatography (SEC) using Waters Alliance GPCV 2000instrument with online viscometer. The oven temperature is 140° C.Trichlorobenzene is used as a solvent (ISO 16014).

In detail: The number average molecular weight (M_(n)), the weightaverage molecular weight (M_(w)) and the molecular weight distribution(MWD) are measured by a method based on ISO 16014-1:2003 and ISO16014-4:2003. A Waters Alliance GPCV 2000 instrument, equipped withrefractive index detector and online viscosimeter was used with3×TSK-gel columns (GMHXL-HT) from TosoHaas and 1,2,4-trichlorobenzene(TCB, stabilized with 200 mg/L 2,6-Di tert butyl-4-methyl-phenol) assolvent at 145° C. and at a constant flow rate of 1 mL/min. 216.5 μL ofsample solution were injected per analysis. The column set wascalibrated using relative calibration with 19 narrow MWD polystyrene(PS) standards in the range of 0.5 kg/mol to 11 500 kg/mol and a set ofwell characterized broad polypropylene standards. All samples wereprepared by dissolving 5-10 mg of polymer in 10 mL (at 160° C.) ofstabilized TCB (same as mobile phase) and keeping for 3 hours withcontinuous shaking prior sampling in into the GPC instrument.

Melt Strength and Melt Extensibility by Rheotens Measurement:

The strain hardening behaviour of polymers is analysed by Rheotensapparatus (product of Göttfert, Siemensstr. 2, 74711 Buchen, Germany) inwhich a melt strand is elongated by drawing down with a definedacceleration. The haul-off force F in dependence of draw-down velocity vis recorded.

The test procedure is performed in a standard climatised room withcontrolled room temperature of T=23° C. The Rheotens apparatus iscombined with an extruder/melt pump for continuous feeding of the meltstrand. The extrusion temperature is 200° C.; a capillary die with adiameter of 2 mm and a length of 6 mm is used and the acceleration ofthe melt strand drawn down is 120 mm/s². The maximum points (F_(max);v_(max)) at failure of the strand are characteristic for the strengthand the drawability of the melt.

Intrinsic viscosity: is measured according to DIN ISO 1628/1, October1999 (in Decalin at 135° C.).

The crosslinked fraction is assumed to be identical to the xylene hotinsoluble (XHI) fraction, which is determined by extracting 1 g offinely cut polymer sample with 500 ml xylene in a Soxleth extractor for48 hours at the boiling temperature. The remaining solid amount is driedat 90° C. and weighed for determining the insolubles amount.

Adhesion

Peel resistance (adhesive bond strength) was determined with the T-PeelTest according to ASTM D 1876-01 using an Instron 4502 tensile tester.

Test samples: extrusion coated UG kraft paper; 5 pieces, cut in machinedirection, 25.4×150 mm. Samples were conditioned for one day at arelative humidity of 50±2% at 23±1° C.

The layers were separated at the desired interface, placed to the armsof the tensile tester and the force required to pull the layers apartwas measured. The result was the force needed for peeling given in N/cm(peel strength in terms of load per unit width of bond line) The peelingtypes are defined as “fiber-tear” (if the propylene composition filmbeing extrusion coated onto the paper substrate is separated from thatpaper takes fibers with it, meaning extremely good adhesion; e.g.cohesive failure in paper) or “no fibers” (no fibers are taken; purepeeling)

EXAMPLES

Materials Used:

-   Component (A): Daploy™ WF420HMS (High melt strength polypropylene    homopolymer; Borealis)-   Component (B):    -   (i) Priex® 25097 (Maleic anhydride grafted polypropylene random        copolymer; Solvay Plastics)    -   (ii) Licocene® PP MA 7452 (Maleic anhydride grafted        polypropylene wax, based on metallocene technology)    -   (iii) BorFlow™ HL504FB (polypropylene homopolymer with MFR of        450 g/10 min, according to ISO 1133, 230° C., 2.16 kg; Borealis)    -   (iv) Sitomelt K608/1 (EVA based hot melt adhesive, Kiilto OY)    -   (v) Primacor™ 3440 (ethylene acrylic acid copolymer, Dow) was        used in a comparative example

Example 1 Preparation of Blends of Component (A) with Component (B)

The compositions were formulated by dry mixing the above describedcommercially available starting materials together and thenmelt-blended. 90 to 95 wt % of WF420HMS were mixed with 5 to 10 wt % ofone of the components (B).

For the Beloit line extrusion coating, the melt-blending was carried outin a Werner&Pfleiderer ZSK40 twin-screw extruder at a temperature of 200to 240° C. (Screw speed was 500 rpm, output was 50 kg/h)

The polymer melt strings from extruder were cooled down in a water bathand dried with air and cut into pellets.

For the Demaq line extrusion coating, the melt blending was done in acompounder BESL 10, Berstorff ZE 25 with capacity of 5-10 kg/h. It hasco-rotating twin-screws, with L/D ratio 40/25. Starting materials wereweighted and dry mixed together before taking them to extruder for meltblending. Set value for melt temperature was 200° C. and temperatureprofile was 195-200-200-200-200-200-200-200, blending was done undernitrogen flush. Set value for screw speed was 200 RPM and for feeders 7kg/h. The polymer melt strings from extruder were cooled down in aroom-temperature water bath and dried with air and cut into pellets.

Example 2-7

Extrusion coating runs were made on Beloit coextrusion coating line.Beloit line had Extruders 1&2 with size of 4,5″ and L/D 24; output was450 kg/h (for LDPE) and Extruder 3 in size of 2,5″ and L/D 30; outputwas 170 kg/h. It had a Peter Cloeren's die and a five layer feed block.The width of the line was 600-800 mm and the maximum line speed was 1000m/min (design value).

In the coating line above a UG kraft paper (UPM Prime Wrap) having abasis weight of 70 g/m² was coated with a co-extruded structure, whichwas composed of 20 g/m² of WF420HMS on the top layer and 20 g/m² ofWF420HMS respectively of blends prepared according to Example 1 in thelayer against paper. Together all coatings had a basis weight of 40g/m². The temperature of the polymer melt was set to 290° C. and theextruders' temperature profile was 200-240-290-290° C. The chill rollwas matt and temperature of its surface was 15° C. Used die opening was0.65 mm and nip distance was 160 mm. Melt film touched the substrate forthe first time+10 mm from nip to substrate side. Pressure of thepressure roll was 3.0 kp/cm². The line speed was 100 m/min.

5 test samples (25.4×150 mm) of WF420HMS coated paper, as well as ofWF420 HMS-blend coated paper were tested regarding adhesion by theT-Peel Test according to ASTM D 1876 on an Instron Tensile Tester.

Results are summarized in Table 1: TABLE 1 Adhesion Test-nopre-treatments Coating material Component(A)/(B) Load Load/widthImprovement Example [wt %] [N] s.d. [N/cm] s.d. [%] 2 WF420HMS[100] 0.730.04 0.29 0.016 0 3 WF420HMS[90]/ 1.56 0.118 0.61 0.046 113 Priex25097[10] 4 WF4200HMS[95]/ 1.71 0.077 0.67 0.030 134 Licocene PP MA 7452[5] 5 WF420HMS[90]/ 0.91 0.083 0.36 0.033 24 BorFlow HL504FB[10] 6WF420HMS[90]/ 1.05 0.048 0.41 0.019 43 Sitomelt K608/1[10] 7WF420HMS[90]/ 0.47 0.048 0.19 0.019 31 35 Primacor 3440[10]Example 7 is a Comparative Examples.d. standard deviationAll samples showed pure peeling, “no fiber” peeling typeImprovement in % is compared to the adhesion value of Example 2 (pureWF42OHMS).

Example 8-13

Extrusion coating runs were made on Beloit coextrusion coating line asdescribed for Examples 2-7.

In the coating line above a UG kraft paper (UPM Prime Wrap) having abasis weight of 70 g/m² was coated with a co-extruded structure, whichwas composed of 20 g/m² of WF420HMS on the top layer and 20 g/m² ofWF420HMS respectively of blends, prepared according to Example 1, in thelayer against paper. Together all coatings had a basis weight of 40g/m². The temperature of the polymer melt was set to 290° C. and theextruders' temperature profile was 200-240-290-290° C. The chill rollwas matt and temperature of its surface was 15° C. Used die opening was0.65 mm and nip distance 160 mm. Melt film touched the substrate for thefirst time +10 mm from nip to substrate side. Pressure of the pressureroll was 3.0 kp/cm². The line speed was 100 m/min.

Ozone treatment for the melt (Sherman) and Corona treatment for thesubstrate (Vetaphone) have been employed for all samples. Sherman ozonetreater had a maximum output power of 4.0 kW and ozone concentrationaround 30 g/m³. Set point for ozone was 2.6 kW and thus concentration ofozone was 19-20 g/m³. Applicator's distance and angle from molten filmwas 70 mm and 45°. Vetaphone ET5 corona treater had a output power of 12kW and frequency of 18 to 35 kHz. It had an HF-amplifier with outputvoltage of 15 to 25 kV and multi-profile aluminium electrode. Set pointfor used corona was 12.0 kW.

5 test samples (25.4×150 mm) of WF420HMS coated paper, as well as ofWF420 HMS-blend coated paper were tested regarding adhesion by theT-Peel Test according to ASTM D 1876 on an Instron Tensile Tester.

Results are summarized in Table 2: TABLE 2 Adhesion Test-ozone andcorona pre-treatment Coating material Component(A)/(B) Load Load/widthImprovement Example [wt %] [N] s.d. [N/cm] s.d. [%] 8 WF420HMS[100] 2.100.109 0.83 0.043 0 9 WF420HMS[90]/ 2.33 0.106 0.92 0.042 10 Priex25097[10] 10 WF420HMS[95]/ 3.51 0.438 1.38 0.173 66 Licocene PP MA7452[5] 11 WF420HMS[90]/ 2.11 0.181 0.83 0.071 0 BorFlow HL504FB[10] 12WF420HMS[90] 3.64 0.803 1.43 0.316 72 Sitomelt K608/1[10] 13WF420HMS/[90]V 1.99 0.093 0.78 0.037 −6 Primacor 3440[10]Example 13 is a Comparative Examples.d. standard deviationSamples 8-11 and sample 13 showed “fiber-tear” peeling type, e.g.cohesive failure in the paperFor Sample 12 the failure was “fiber-tear” for 2 of 5 pieces and “nofiber” for 3 of 5 pieces.Improvement in % is compared to the adhesion value of Example 8(pureWF420HMS).

Example 14-19

Extrusion coating runs were made on a Demag coating line. It was a castfilm line adapted to extrusion coating. The nip configuration differedfrom conventional extrusion coating line's horizontal die placing by thedie being in 45° angle from horizontal direction; however the moltenfilm was coming to the nip tangential to chill roll as normally. Demaqline had an extruder with L/D ratio 45/31 and maximum output was 60kg/h. There were no back pressure valves in Demaq. The die was aUltraflex R75 450 mm (Extrusion Dies Inc.). The maximum width of thepaper roll for the line was 420 mm and the maximum line speed was 200m/min (design value). Chill roll was glossy and maximum pressure forpressure roll was 6 bar.

In the coating line above a UG kraft paper (UPM Prime Wrap) having abasis weight of 70 g/m² was coated in monolayer structures with a layerof WF420HMS, respectively of blends prepared according to Example 1, allhaving a basis weight of 40 g/m². The temperature of the polymer meltwas set to 290° C. The line speed was 20 m/min. Die opening was 0.5 mm,nip distance 170 mm and nip pressure 6 bar.

5 test samples (25.4×150 mm) of WF420HMS coated paper, as well as ofWF420 HMS-blend coated paper were tested regarding adhesion by theT-Peel Test according to ASTM D 1876 on an Instron Tensile Tester.

Results are summarized in Table 3: TABLE 3 Adhesion Test-nopre-treatments Coating material Component(A)/(B) Load Load/widthImprovement Example [wt %] [N] s.d. [N/cm] s.d. [%] 14 WF420HMS[100]1.426 0.216 0.56 0.085 0 15 WF420HMS[90]/ 1.916 0.145 0.75 0.057 34Priex 25097[10] 16 WF42OHMS[90]/ 4.986 0.235 1.956 0.093 249 Licocene PPMA 7452[10] 17 WE42OHMS[90]/ 1.901 0.217 0.75 0.086 33 BarFlowHL504FB[10] 18 WF420HMS[90]/ 1.927 0.123 0.76 0.049 35 SitomeltK608/1[10] 19 WF420HMS[90]/ 1.132 0.198 0.45 0.078 −21 Primacor 3440[10]Example 19 is a Comparative Examples.d. standard deviationImprovement in % is compared to the adhesion value of Example 14 (pureWF420HMS).

1. Two-component adhesion composition suitable for extrusion coatingpaper substrates comprising a) from 70 to 98 wt % of high melt strengthpolypropylene (A) with a branching index g′ of 0.9 or less, wherein thecross-linked fraction of the polypropylene (A) does not exceed 1.0wt.-%, determined as the relative amount of polymer insoluble in boilingxylene (xylene hot insoluble fraction, XHI) and b) from 2 to 30 wt % ofa component (B) selected from the group of (i) maleic anhydride-modifiedpolypropylene (MAPP) or (ii) maleic anhydride-modified polypropylenewax.
 2. Composition according to claim 1, wherein the high melt strengthpolypropylene (A) is a propylene homopolymer.
 3. Composition accordingto claim 1, wherein the high melt strength polypropylene (A) has beenobtained by treating an unmodified polypropylene (A′) with a peroxideand optionally with a bifunctional monomer.
 4. Composition according toclaim 1, wherein the maleic anhydride-modified polypropylene (i) is arandom copolymer of propylene and ethylene.
 5. Composition according toclaim 1, wherein the maleic anhydride-modified polypropylene (i) has acontent of maleic anhydride in the modified polypropylene in the rangeof 0.001 to 10 wt %, based on the weight of the modified polypropylene.6. Composition according to claim 1, wherein the maleicanhydride-modified polypropylene wax (ii) has been obtained by graftingan unmodified polypropylene wax, which was prepared in the presence of ametallocene catalyst.
 7. Composition according to claim 1, wherein themaleic anhydride-modified polypropylene wax (ii) has been obtained bygrafting an unmodified polypropylene wax, which had a weight averagemolecular weight (Mw) of the polypropylene waxes of less than 10,000g/mol.
 8. Composition according to claim 1, wherein the maleicanhydride-modified polypropylene wax (ii) has a content of maleicanhydride in the modified polypropylene wax in the range of 0.1 to 20 wt% based on the weight of the modified polypropylene.
 9. (canceled) 10.(canceled)
 11. (canceled)
 12. (canceled)
 13. Extrusion coating processusing paper as substrate and using the polypropylene compositionaccording to claim
 1. 14. Extrusion coated article comprising a papersubstrate and at least one layer of the propylene polymer compositionaccording to claim 1 on at least one surface of the article.
 15. Anarticle according to claim 14 which is a packaging material. 16.Composition according to claim 2, wherein the high melt strengthpolypropylene (A) has been obtained by treating an unmodifiedpolypropylene (A′) with a peroxide and optionally with a bifunctionalmonomer.
 17. Two-component adhesion composition suitable for extrusioncoating paper substrates comprising a) from 70 to 98 wt % of high meltstrength polypropylene (A) with a branching index g′ of 0.9 or less andb) from 2 to 30 wt % of a component (B) selected from the group of (iii)polypropylene homopolymer with high melt flow rate or (iv)ethylene-vinyl acetate-based hot melt adhesive.
 18. Compositionaccording to claim 17, wherein the high melt strength polypropylene (A)is a propylene homopolymer.
 19. Composition according to claim 17,wherein the high melt flow rate polypropylene homopolymer (iii) has amelt flow rate measured according to ISO 1133 at 230° C. under a load of2.16 kg of from 50 to 3000 g/10 min.
 20. Composition according to claim17, wherein the high melt flow rate polypropylene homopolymer (iii) hasbeen obtained by a controlled rheology technology using organicperoxides.
 21. Composition according to claim 17, wherein theethylene-vinyl acetate-based hot melt adhesive (iv) containsethylene-vinyl acetate-copolymers with 15 to 45 wt % vinyl acetate andhaving a melt index (ISO 1133, 190° C., 2.16 kg) in the range of 2 to2500 g/10 min.
 22. Extrusion coating process using paper as substrateand using the polypropylene composition according to claim
 17. 23.Extrusion coated article comprising a paper substrate and at least onelayer of the propylene polymer composition according to claim 17 on atleast one surface of the article.
 24. An article according to claim 23which is a packaging material.
 25. Composition according to claim 17,wherein the maleic anhydride-modified polypropylene (i) is a randomcopolymer of propylene and ethylene.